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1.
Mol Cell Probes ; 17(4): 171-4, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12944119

ABSTRACT

Evidence is presented demonstrating that the distribution of data obtained applying a given RT-PCR method deviates from a normal distribution depending on the limit of detection. The effect of this is a bias towards higher values and concomitantly a systematic error in respect to the accuracy of the evaluation due to this deviation from normality. In addition, evidence is presented that an evaluation assuming a log-normal distribution is more appropriate.


Subject(s)
Data Interpretation, Statistical , Hepatitis A virus/genetics , RNA, Viral/analysis , RNA/analysis , Reverse Transcriptase Polymerase Chain Reaction/standards , Hepatitis A virus/isolation & purification , Humans , Normal Distribution , Reference Values , Reproducibility of Results
2.
J Virol ; 77(12): 7017-25, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12768020

ABSTRACT

Recombinant vaccinia viruses that express defective retroviral vectors upon a single infection event in normal host cells were constructed. The gag-pol and envelope genes and a retroviral vector unit were inserted as vaccinia virus promoter-controlled transcription units at three separate loci. The triple recombinant virus was used to infect such diverse cell types as monkey and rabbit kidney, human lung, and primary chicken cells, resulting in the production of transduction-competent defective retroviral vectors. Infection of Chinese hamster ovary cells, which are nonpermissive for vaccinia virus replication, also resulted in production of retroviral vectors and secondary permanent transduction of the host cells. Since vaccinia virus supports the expression of cytotoxic proteins, the vesicular stomatitis virus G glycoprotein could be chosen as the envelope allowing a broad host range of transduction. Functionality of particles was monitored by expression of the green fluorescent protein in transduced 3T3 cell clones. This is the first description of a single chimeric virus encoding and releasing functional retroviral vectors, providing proof of principle of the new concept. No replication-competent retrovirus was detectable by sensitive reverse transcriptase assays. Since vaccinia virus has a broad host range, is extremely robust, and can be obtained at high titers and safe nonreplicating vaccinia virus strains are available, the hybrid system may open new perspectives for gene delivery.


Subject(s)
Genetic Vectors , Recombination, Genetic , Retroviridae/genetics , Transduction, Genetic , Vaccinia virus/genetics , 3T3 Cells , Animals , CHO Cells , Cell Line , Chlorocebus aethiops , Cricetinae , Humans , Membrane Glycoproteins/genetics , Mice , Rabbits , Retroviridae/physiology , Vaccinia virus/physiology , Vero Cells , Viral Envelope Proteins/genetics , Virus Replication
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